此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Effect of Remote Ischemic Conditioning in Patients With Chronic Ischemic Heart Failure (CONDI-HF)

2017年8月23日 更新者:University of Aarhus

Effect of Remote Ischemic Conditioning in Patients With Chronic Ischemic Heart Failure (CONDI-HF)

The present study will evaluate whether treatment with daily remote ischemic conditioning for a 28±4-day period induces beneficial effects in subjects with and without chronic ischemic heart failure in terms of improved left ventricular contractile function and exercise capacity.

研究概览

详细说明

Background Chronic heart failure (CHF) is a leading cause of morbidity and mortality throughout the world, and the incidence and prevalence are increasing as more patients survive their acute coronary syndrome. The disease is caused by abnormalities in cardiac structure or function leading to insufficient delivery of oxygen to the metabolizing tissues. These patients are often debilitated, require chronic medications, and many receive expensive device therapy to manage symptoms. Consequently, this has led to an increasing economic and health burden from heart failure.

CHF is the end-stage of a broad range of underlying cardiovascular diseases, but is most frequently caused by ischemic heart disease. Other contributory causes include hypertension, heart valve diseases, arrhythmias and cardiomyopathies, all resulting in myocardial tissue damage and loss of ventricular function. Activation of neurohormonal and inflammatory compensatory mechanisms lead to a vicious circle through adaptive metabolic and remodeling processes, eventually resulting in a progressive decline of cardiac function with significant morbidity and mortality.

Identification of the specific underlying cardiac condition is crucial for the therapeutic approach in patients suffering from CHF. While pharmacological treatment remains dominating, resynchronization therapy and surgical resection of non-contractile tissue are also increasingly being conducted. Despite the fact that activation of the inflammatory system greatly contributes to the remodeling process through initiation of myocardial fibrosis and hypertrophy, most clinical studies targeting inflammatory components have been discouraging.

Remote ischemic conditioning (RIC) by brief non-lethal episodes of ischemia in a remote organ or tissue (e.g. a limb) is a novel therapeutic method to achieve protection against ischemia-reperfusion injury in the target organ, e.g. the heart . In the clinical setting, RIC is most often performed by repeated episodes of limb ischemia achieved by intermittent inflation of a blood pressure cuff placed around the upper arm. In clinical randomized trials, RIC has been shown to reduce the amount of myocardial injury and improve long-term outcome in patients admitted with STEMI for primary percutaneous coronary intervention and patients undergoing cardiac surgery or elective coronary intervention.

RIC is a low-cost, simple and safe procedure that can easily be conducted using a standard blood pressure cuff, and the method is increasingly used in clinical trials. The mechanisms behind RIC are not yet fully understood, but the cardioprotective effects are believed to be caused by neural and humoral signaling cascades as well as systemic anti-inflammatory effects resulting in a cytoprotective state. In addition, RIC has been shown to reduce thrombus formation. Since activation of platelets and the coagulation system are fundamental in thrombus formation and degradation, another possible mechanism of the described effects of RIC could be a result from effect on arterial thrombus formation.

The vast majority of experimental and clinical studies have utilized RIC as single-occasion treatment (i.e. 3 or 4 bouts of short limb ischemia conducted once). However, experimental studies have recently suggested that repeated RIC treatment may infer further beneficial effects. Repeated RIC application has been shown to improve endothelial function and modify leukocyte adhesion in healthy volunteers. In a rat model of myocardial infarction, RIC repeated daily for 28 days after infarction reduced adverse ventricular remodeling and improved survival. Consequently, two on-going clinical trials (clinicaltrials.gov: DREAM study NCT01664611 and CRIC-RCT study NCT01817114) are investigating the effect of repeated RIC on LVEF function in patients with reduced ventricular function after an acute coronary event. Another study investigates the effect of repeated RIC on patients with severe heart failure and left ventricular assist device (IMPULSE study NCT02044471).

So far, the effect of RIC on patients suffering from stable chronic ischemic heart failure is unknown. Furthermore, no registered studies have evaluated the effect of long-term RIC given as additive treatment to the standard medical therapy in patients with chronic ischemic heart failure.

Hypothesis

• We hypothesize, that the combination of anti-remodelling and anti-inflammatory properties together with improved endothelial function induced by repetitive RIC treatment translate into improved left ventricular function and better physical performance in subjects with CHF.

Purpose

  • To determine whether RIC applied on a daily basis for 4 weeks improves left ventricular function as assessed by cardiac magnetic resonance imaging (MRI) in subjects with CHF.
  • To investigate whether RIC applied on a daily basis for 4 weeks improves muscle strength, cardiopulmonary exercise capacity and thrombocyte function, and changes blood biomarker levels of inflammation and heart failure in subjects with CHF.
  • To investigate whether the above-mentioned measurements differ between patients with CHF and matched subjects after RIC applied on a daily basis for 4 weeks.

Perspectives The present study will elucidate whether long-term RIC treatment induces beneficial effects in subjects with and without chronic ischemic heart failure in terms of improved left ventricular contractile function and exercise capacity, and whether long-term RIC treatment induces systemic anti-inflammatory effects in these subjects. Moreover, we find that the study can uncover some of the mechanisms behind RIC and thus potentially optimize future treatment for patients suffering, or at risk, from ischemic heart diseases.

研究类型

介入性

注册 (实际的)

47

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • DK-8200 Aarhus N
      • Aarhus N、DK-8200 Aarhus N、丹麦、8200
        • Aarhus University Hospital Skejby

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Group 1 (Chronic heart failure patients):

Inclusion Criteria:

  • >18 years of age
  • Able to understand the written patient information and to give informed consent
  • Chronic congestive ischemic heart failure
  • Left ventricular ejection fraction ≤45%
  • New York Heart Association functional class I-III

Exclusion Criteria:

  • Recent cardiovascular hospitalization (within last 30 days) • Strenuous exercise within 72 hours of either study visits
  • Intake of caffeine within 24 hours of either study visit
  • Intake of alcohol within 24 hours of either study visit
  • Patients with permanent atrial fibrillation • Patients with diabetes mellitus
  • Patients with peripheral neuropathy
  • Patients in dialysis treatment
  • Contraindication for Magnetic Resonance Imaging examination (e.g. metal implants including Cardiac Resynchronisation Therapy devices and other pacemakers or defibrillators) precluding Magnetic Resonance Imaging
  • Other concomitant disease or treatment that according to the investigator's assessment makes the patient unsuitable for study participation.

Group 2 (Volunteers without ischemic heart disease):

Inclusion criteria:

  • >18 years of age
  • Able to understand the written patient information and to give informed consent
  • Left ventricular ejection fraction >45%

Exclusion criteria:

  • Recent cardiovascular hospitalization (within last 30 days)
  • Intake of acetylsalicylic acid or non-steroidal anti-inflammatory drug medication within 7 days of either study visit
  • Strenuous exercise within 72 hours of either study visit
  • Intake of caffeine within 24 hours of either study visit
  • Intake of alcohol within 24 hours of either study visit
  • Patients with ischemic heart disease
  • Patients with diabetes mellitus
  • Patients with peripheral neuropathy
  • Patients in dialysis treatment
  • Patients in treatment with Vitamin K-antagonists, adenosine diphosphate-receptor-inhibitor, oral anticoagulants or dipyridamol.
  • Conditions contraindicating short term cessation of acetylsalicylic acid and/or non-steroidal anti-inflammatory drug intake
  • Contraindication for Magnetic Resonance Imaging examination (e.g. metal implants) precluding Magnetic Resonance Imaging
  • Other concomitant disease or treatment that according to the investigator's assessment makes the patient unsuitable for study participation.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Daily RIC
Daily ischemic conditioning treatment
RIC stimulus will be conducted as 4 x 5 minutes upper arm ischemia achieved by inflation of a blood pressure cuff to 200 mmHg and 5 minutes reperfusion between inflations. The procedure will be performed using the AutoRICTM (CellAegis Devices Inc., Toronto, Ontario, Canada).

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Left ventricular ejection fraction assessed by MRI
大体时间:28±4 days
28±4 days

次要结果测量

结果测量
大体时间
Global and regional myocardial function by strain analysis assessed by MRI
大体时间:28±4 days
28±4 days
Left ventricular mass and end-diastolic volume assessed by MRI
大体时间:28±4 days
28±4 days
Cardiac output assessed by MRI
大体时间:28±4 days
28±4 days
Cardiopulmonary exercise capacity assessed by staged exercise bicycle test and leg extension power rig test
大体时间:28±4 days
28±4 days
Serology markers for heart failure
大体时间:28±4 days
28±4 days
Serology inflammatory markers
大体时间:28±4 days
28±4 days

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 研究主任:Hans Erik Bøtker, Prof.、Department of cardiology, Aarhus University Hospital

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2014年9月1日

初级完成 (实际的)

2016年2月1日

研究完成 (实际的)

2016年2月1日

研究注册日期

首次提交

2014年9月2日

首先提交符合 QC 标准的

2014年9月24日

首次发布 (估计)

2014年9月25日

研究记录更新

最后更新发布 (实际的)

2017年8月24日

上次提交的符合 QC 标准的更新

2017年8月23日

最后验证

2016年10月1日

更多信息

与本研究相关的术语

其他研究编号

  • VEK: 1-10-72-173-14

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅